6243 - Downstream Principal Engineer / Lead Validation Engineer

Verista; Holly Springs (NC); On-site; USD 108,000 - 168,000; Full time

Benefits offered by this job

Competitive pay plus performance-based

Company-paid Insurance: Life, STD, LTD

Medical, Dental & Vision Insurance

401(k) with employer match

Paid Time Off and Holidays

Tuition Reimbursement

Team Social Activities

Employee Recognition

Employee Referral Program

Paid Parental Leave and Bereavement

Job summary

Verista is seeking a Downstream Principal Engineer to oversee commissioning and qualification of downstream systems in a GMP-biopharma environment. You will lead C&Q activities, review engineering docs, develop URS/QRAES, IOQ, and test plans while coordinating with design engineers and SMEs.

Role requires 10+ years of CQV experience, hands-on downstream equipment knowledge, and strong documentation. Onsite in Holly Springs, NC with competitive pay and comprehensive benefits.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, Biotechnology, or related technical discipline.
• 10+ years of role-specific experience in CQV for GMP-regulated biotech/pharma.
• Hands-on experience with downstream bioprocess equipment and purification systems.
• Strong documentation, organizational, and communication skills.
• Experience with FAT/SAT, commissioning and equipment startup.

Responsibilities

• Oversee commissioning and qualification of downstream systems.
• Lead C&Q activities and ensure alignment with project requirements and safety standards.
• Develop URS, QRAES, IOQ protocols, test plans, and summary reports.
• Collaborate with design engineers, SMEs, automation teams, and QA to ensure testability and traceability.
• Provide system ownership post-construction and manage risk-based validation approaches.
• Support FAT/SAT and site acceptance tests as required.

Skills

CQV experience

Independent working

Documentation skills

Validation lifecycle

Kneat experience

FAT/SAT exposure

Risk-based validation

Biologics manufacturing know-how

Downstream equipment

Education

Bachelor’s degree in Engineering, Life Sciences, Biotechnology, or related technical discipline

Tools

Kneat

Job description

Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities. Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do the right thing
• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

We are seeking a Downstream Principal Engineer is responsible for overseeing the commissioning and qualification of downstream systems. This role ensures that all systems are designed, tested, and documented in alignment with project requirements and safety standards.

Downstream Principal Engineer Responsibilities:

Downstream System Leadership

• Serve as the commissioning and qualification lead for Downstream systems (responsibilities described below).
• Specific experience with chromatography systems, TFF filtration systems, viral filtration systems, and UFDF filtration systems.

C&Q Lead Responsibilities

Commissioning and Qualification Documentation

• Gain a thorough understanding of system design by reviewing engineering documentation, P&IDs, and design specifications.
• Develop User Requirement Specifications (URS) and Quality Risk Assessment for Equipment and Automated Systems (QRAES).
• Engage with design engineers and SMEs to clarify system intent and operational requirements.
• Ensure alignment with quality, automation, and engineering teams on critical parameters and documentation.
• Create Commissioning Test Plans that translate design intent into testable steps.
• Coordinate with the Automation Team to incorporate all automation functional testing.
• Collaborate with SMEs to ensure system requirements are accurately reflected in test plans.
• Develop Installation, Operational, and Qualification (IOQ) protocols.
• Prepare and submit summary reports documenting commissioning and qualification activities.

System Ownership and Execution

• Take custody of the system post-construction and maintain ownership through C&Q completion.
• Perform Lockout/Tagout (LOTO) for system safety.
• Conduct pre-startup safety checks and risk assessments.
• Prepare daily pre-task plans and verify team readiness for safe execution.
• Attend daily commissioning meetings to coordinate activities.
• Execute commissioning and IOQ protocols.
• Resolve issues arising during execution.
• Participate in Factory Acceptance Tests (FATs) and Site Acceptance Tests (SATs) as required.

Requirements:

• Bachelor’s degree in Engineering, Life Sciences, Biotechnology, or related technical discipline
• 10+ years of role specific experience
• Experience supporting CQV activities in GMP-regulated pharmaceutical or biotechnology environments
• Hands-on experience with downstream bioprocess equipment and purification systems
• Strong understanding of validation lifecycle documentation (IQ/OQ/PQ, protocols, reports)
• Ability to work independently while collaborating with cross-functional teams
• Strong documentation, organizational, and communication skills
• Experience with digital validation systems such as Kneat
• Experience supporting FAT/SAT, commissioning, and equipment startup
• Familiarity with risk-based validation approaches
• Experience in biologics manufacturing or monoclonal antibody production environments
• Onsite job requirement in Holly Springs, NC

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.*Verista is an equal opportunity employer.

National (US) Range: $107,800 USD - $168,011 USD

Benefits

Why Choose Verista?

• High growth potential and fast-paced organization with a people-focused culture
• Competitive pay plus performance-based incentive programs
• Company-paid Life, Short-Term, and Long-Term Disability Insurance.
• Medical, Dental & Vision insurances
• FSA, DCARE, Commuter Benefits
• Supplemental Life, Hospital, Critical Illness and Legal Insurance
• Health Savings Account
• 401(k) Retirement Plan (Employer Matching benefit)
• Paid Time Off (Rollover Option) and Holidays
• As Needed Sick Time
• Tuition Reimbursement
• Team Social Activities (We have fun!)
• Employee Recognition
• Employee Referral Program
• Paid Parental Leave and Bereavement

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For more information about our company, please visit us at Verista.com